176 related articles for article (PubMed ID: 18539994)
1. Diffuse multicystic encephalomalacia in a preterm baby due to homozygous methylenetetrahydrofolate reductase 677 C-->T mutation.
Aygun C; Tanyeri B; Ceyhan M; Bagci H; Kucukoduk S
J Child Neurol; 2008 Jun; 23(6):695-8. PubMed ID: 18539994
[TBL] [Abstract][Full Text] [Related]
2. Maternal mutation 677C > T in the methylenetetrahydrofolate reductase gene associated with severe brain injury in offspring.
Dodelson de Kremer R; Grosso C
Clin Genet; 2005 Jan; 67(1):69-80. PubMed ID: 15617551
[TBL] [Abstract][Full Text] [Related]
3. Prevention of brain disease from severe 5,10-methylenetetrahydrofolate reductase deficiency.
Strauss KA; Morton DH; Puffenberger EG; Hendrickson C; Robinson DL; Wagner C; Stabler SP; Allen RH; Chwatko G; Jakubowski H; Niculescu MD; Mudd SH
Mol Genet Metab; 2007 Jun; 91(2):165-75. PubMed ID: 17409006
[TBL] [Abstract][Full Text] [Related]
4. Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiency.
Baethmann M; Wendel U; Hoffmann GF; Göhlich-Ratmann G; Kleinlein B; Seiffert P; Blom H; Voit T
Neuropediatrics; 2000 Dec; 31(6):314-7. PubMed ID: 11508552
[TBL] [Abstract][Full Text] [Related]
5. Severe methylenetetrahydrofolate reductase (MTHFR) deficiency: a case report of nonclassical homocystinuria.
Bishop L; Kanoff R; Charnas L; Krenzel C; Berry SA; Schimmenti LA
J Child Neurol; 2008 Jul; 23(7):823-8. PubMed ID: 18658082
[TBL] [Abstract][Full Text] [Related]
6. Methylenetetrahydrofolate reductase 677CT polymorphism and cobalamin, folate, and homocysteine status in Spanish adolescents.
Al-Tahan J; Sola R; Ruiz JR; Breidenassel C; García-Fuentes M; Moreno LA; Castillo M; Pietrzik K; González-Gross M
Ann Nutr Metab; 2008; 52(4):315-21. PubMed ID: 18714149
[TBL] [Abstract][Full Text] [Related]
7. Influence of methylenetetrahydrofolate reductase gene polymorphisms on homocysteine concentrations after nitrous oxide anesthesia.
Nagele P; Zeugswetter B; Wiener C; Burger H; Hüpfl M; Mittlböck M; Födinger M
Anesthesiology; 2008 Jul; 109(1):36-43. PubMed ID: 18580170
[TBL] [Abstract][Full Text] [Related]
8. Methylenetetrahydrofolate reductase deficiency and low dietary folate reduce tumorigenesis in Apc min/+ mice.
Lawrance AK; Deng L; Rozen R
Gut; 2009 Jun; 58(6):805-11. PubMed ID: 19174418
[TBL] [Abstract][Full Text] [Related]
9. Severe purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation.
Demirel N; Bas AY; Okumus N; Zenciroglu A; Yarali N
Pediatr Hematol Oncol; 2009 Nov; 26(8):597-600. PubMed ID: 19954370
[No Abstract] [Full Text] [Related]
10. Thrombophilia and fetal germinal matrix-intraventricular hemorrhage: does it matter?
Ramenghi LA; Fumagalli M; Righini A; Triulzi F; Kustermann A; Mosca F
Ultrasound Obstet Gynecol; 2005 Oct; 26(5):574-6. PubMed ID: 16184507
[TBL] [Abstract][Full Text] [Related]
11. [Diagnostic contribution of the electroencephalogram in the premature infant: personal casuistry (author's transl)].
Ferrari F
Pediatr Med Chir; 1981; 3(6):495-505. PubMed ID: 7343947
[No Abstract] [Full Text] [Related]
12. Neonatal antiphospholipid syndrome associated with heterozygous methylentetrahydrofolate reductase C677T and prothrombin G20210A gene mutations.
Paro-Panjan D; Kitanovski L; Avcin T
Rheumatology (Oxford); 2007 Apr; 46(4):720-1. PubMed ID: 17307756
[No Abstract] [Full Text] [Related]
13. Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients.
Forges T; Chery C; Audonnet S; Feillet F; Gueant JL
Mol Genet Metab; 2010 Jun; 100(2):143-8. PubMed ID: 20356773
[TBL] [Abstract][Full Text] [Related]
14. Posterior cerebral artery occlusion after Mycoplasma pneumoniae infection associated with genetic defect of MTHFR C677T.
Ryu JS; Kim HJ; Sung IY; Ko TS
J Child Neurol; 2009 Jul; 24(7):891-4. PubMed ID: 19617462
[TBL] [Abstract][Full Text] [Related]
15. [Multiple cerebral infarcts with resulting multicystic encephalomalacia in a premature infant with Enterobacter sakazakii meningitis].
Ries M; Harms D; Scharf J
Klin Padiatr; 1994; 206(3):184-6. PubMed ID: 8051914
[TBL] [Abstract][Full Text] [Related]
16. Differences in liver folate enzyme patterns in premature and full term infants.
Kalnitsky A; Rosenblatt D; Zlotkin S
Pediatr Res; 1982 Aug; 16(8):628-31. PubMed ID: 7050870
[TBL] [Abstract][Full Text] [Related]
17. Two Aspergillus nidulans genes encoding methylenetetrahydrofolate reductases are up-regulated by homocysteine.
Sieńko M; Natorff R; Zieliński Z; Hejduk A; Paszewski A
Fungal Genet Biol; 2007 Jul; 44(7):691-700. PubMed ID: 17257865
[TBL] [Abstract][Full Text] [Related]
18. Association of homocysteinemia with high concentrations of serum insulin and uric acid in Brazilian subjects with metabolic syndrome genotyped for C677T polymorphism in the methylenetetrahydrofolate reductase gene.
Uehara SK; Rosa G
Nutr Res; 2008 Nov; 28(11):760-6. PubMed ID: 19083485
[TBL] [Abstract][Full Text] [Related]
19. Arterial ischemic stroke in a child with beta-thalassemia trait and methylentetrahydrofolate reductase mutation.
Brankovic-Sreckovic V; Milic Rasic V; Djordjevic V; Kuzmanovic M; Pavlovic S
J Child Neurol; 2007 Feb; 22(2):208-10. PubMed ID: 17621484
[TBL] [Abstract][Full Text] [Related]
20. Altered expression of methylenetetrahydrofolate reductase modifies response to methotrexate in mice.
Celtikci B; Leclerc D; Lawrance AK; Deng L; Friedman HC; Krupenko NI; Krupenko SA; Melnyk S; James SJ; Peterson AC; Rozen R
Pharmacogenet Genomics; 2008 Jul; 18(7):577-89. PubMed ID: 18551038
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
